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Periprocedural bridging therapy in patients receiving chronic oral anticoagulation therapy

Alex C Spyropoulos1, Rupert M Bauersachs, Heyder Omran

  • 1Clinical Thrombosis Center, Lovelace Medical Center, Albuquerque, NM 87108, USA. alex.spyropoulos@lovelacesandia.com

Insights

For patients on vitamin K antagonists (VKAs) needing procedures, bridging therapy with unfractionated heparin (UFH) or low-molecular-weight heparin (LMWH) is recommended for those at high risk of thromboembolism. LMWH offers advantages in administration and cost-effectiveness.

Area of Science:

  • Cardiology
  • Hematology
  • Pharmacology

Background:

  • Patients on chronic anticoagulation with vitamin K antagonists (VKAs) face a bleeding risk during procedures if VKA therapy continues.
  • Discontinuing VKAs increases the risk of thromboembolism, creating a clinical dilemma.

Purpose of the Study:

  • To review periprocedural bridging therapy in patients on chronic oral anticoagulation requiring temporary VKA discontinuation.
  • To evaluate the efficacy and safety of unfractionated heparin (UFH) and low-molecular-weight heparin (LMWH) as bridging therapies.

Main Methods:

  • Systematic narrative review of studies involving patients on chronic oral anticoagulation.
  • Analysis of periprocedural bridging therapy with heparin during invasive procedures.

Main Results:

  • Low-molecular-weight heparins (LMWHs) show low rates of thromboembolism and are as effective and safe as UFH for bridging therapy.
  • LMWHs offer easier administration, predictable effects, and cost savings in outpatient settings compared to UFH.
  • Current guidelines recommend UFH or LMWH for intermediate-to-high thromboembolic risk patients needing VKA interruption.

Conclusions:

  • Bridging therapy decisions require balancing thromboembolism and bleeding risks.
  • Recommend therapeutic doses of UFH or LMWH for high thromboembolic risk patients, especially with low bleeding risk procedures.
  • Propose upgrading ACCP guideline recommendations; further randomized controlled trials are needed to compare bridging strategies.
Abstract

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